JP5588839B2 - 官能化された、完全にまたは部分的に水素化されたニトリルゴムの微粒子の安定な懸濁液 - Google Patents
官能化された、完全にまたは部分的に水素化されたニトリルゴムの微粒子の安定な懸濁液 Download PDFInfo
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- JP5588839B2 JP5588839B2 JP2010257823A JP2010257823A JP5588839B2 JP 5588839 B2 JP5588839 B2 JP 5588839B2 JP 2010257823 A JP2010257823 A JP 2010257823A JP 2010257823 A JP2010257823 A JP 2010257823A JP 5588839 B2 JP5588839 B2 JP 5588839B2
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- Prior art keywords
- suspension
- nitrile rubber
- carboxylated
- fully
- partially hydrogenated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000008346 aqueous phase Substances 0.000 claims description 31
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- 239000000463 material Substances 0.000 claims description 28
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- 238000004519 manufacturing process Methods 0.000 claims description 20
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 46
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- 238000012360 testing method Methods 0.000 description 15
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- 150000002763 monocarboxylic acids Chemical class 0.000 description 6
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- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- 239000004952 Polyamide Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
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- 238000004220 aggregation Methods 0.000 description 5
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- 229920002647 polyamide Polymers 0.000 description 5
- 230000003068 static effect Effects 0.000 description 5
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
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- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- 238000010626 work up procedure Methods 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
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- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- 125000005119 alkyl cycloalkyl group Chemical group 0.000 description 3
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- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
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- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 3
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- VIWNJEGFWMACBY-UHFFFAOYSA-L lithium sodium phosphoric acid carbonate Chemical compound C([O-])([O-])=O.[Li+].P(=O)(O)(O)O.[Na+] VIWNJEGFWMACBY-UHFFFAOYSA-L 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000011089 mechanical engineering Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- SINFYWWJOCXYFD-UHFFFAOYSA-N methoxymethyl prop-2-enoate Chemical compound COCOC(=O)C=C SINFYWWJOCXYFD-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229940074369 monoethyl fumarate Drugs 0.000 description 1
- NKHAVTQWNUWKEO-NSCUHMNNSA-N monomethyl fumarate Chemical compound COC(=O)\C=C\C(O)=O NKHAVTQWNUWKEO-NSCUHMNNSA-N 0.000 description 1
- 229940005650 monomethyl fumarate Drugs 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- SMBYUOXUISCLCF-UHFFFAOYSA-N n-ethyl-n-methylpropan-1-amine Chemical compound CCCN(C)CC SMBYUOXUISCLCF-UHFFFAOYSA-N 0.000 description 1
- XCVNDBIXFPGMIW-UHFFFAOYSA-N n-ethylpropan-1-amine Chemical compound CCCNCC XCVNDBIXFPGMIW-UHFFFAOYSA-N 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical class CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 150000003139 primary aliphatic amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000012783 reinforcing fiber Substances 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Chemical class 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical class [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 238000010092 rubber production Methods 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 229910052719 titanium Chemical class 0.000 description 1
- 239000010936 titanium Chemical class 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000005199 ultracentrifugation Methods 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- XKMZOFXGLBYJLS-UHFFFAOYSA-L zinc;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C=C XKMZOFXGLBYJLS-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/02—Copolymers with acrylonitrile
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
- C08J3/07—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media from polymer solutions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/02—Copolymers with acrylonitrile
- C08L9/04—Latex
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D109/00—Coating compositions based on homopolymers or copolymers of conjugated diene hydrocarbons
- C09D109/02—Copolymers with acrylonitrile
- C09D109/04—Latex
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/18—Homopolymers or copolymers of nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2309/00—Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
- C08J2309/02—Copolymers with acrylonitrile
- C08J2309/04—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2313/00—Characterised by the use of rubbers containing carboxyl groups
- C08J2313/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2315/00—Characterised by the use of rubber derivatives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Dispersion Chemistry (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09176534.7 | 2009-11-19 | ||
| EP09176534A EP2325237A1 (de) | 2009-11-19 | 2009-11-19 | Feinteilige stabile Suspensionen funktionalisierter, ganz oder teilweise hydrierter Nitrilkautschuke |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011105939A JP2011105939A (ja) | 2011-06-02 |
| JP2011105939A5 JP2011105939A5 (de) | 2013-11-07 |
| JP5588839B2 true JP5588839B2 (ja) | 2014-09-10 |
Family
ID=42107399
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010257823A Expired - Fee Related JP5588839B2 (ja) | 2009-11-19 | 2010-11-18 | 官能化された、完全にまたは部分的に水素化されたニトリルゴムの微粒子の安定な懸濁液 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US8642687B2 (de) |
| EP (2) | EP2325237A1 (de) |
| JP (1) | JP5588839B2 (de) |
| KR (1) | KR101818240B1 (de) |
| CN (1) | CN102070802B (de) |
| BR (1) | BRPI1004995A2 (de) |
| CA (1) | CA2721408A1 (de) |
| MX (1) | MX2010012609A (de) |
| RU (1) | RU2559464C9 (de) |
| TW (1) | TWI485188B (de) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8752626B2 (en) * | 2011-12-16 | 2014-06-17 | Halliburton Energy Services, Inc. | Compositions and methods for treatment of well bore tar |
| CN102850850B (zh) * | 2012-09-11 | 2014-08-13 | 东莞市锐达涂料有限公司 | 一种酯溶淋膜复合油墨 |
| EP2868676A1 (de) * | 2013-10-30 | 2015-05-06 | LANXESS Deutschland GmbH | Funktionalisierter nitrilgruppenhaltiger Copolymerkautschuk |
| SG11201700561WA (en) * | 2014-07-24 | 2017-02-27 | Arlanxeo Singapore Pte Ltd | Ultrapure copolymers |
| EP3239265B1 (de) * | 2014-12-26 | 2019-07-10 | Zeon Corporation | Latex für reibungsmaterial und reibungsmaterial |
| JP6537215B2 (ja) * | 2015-09-25 | 2019-07-03 | エルジー・ケム・リミテッド | カーボンブラック分散液およびその製造方法 |
| EP3385090B1 (de) * | 2017-04-04 | 2019-12-25 | Continental Reifen Deutschland GmbH | Verfahren zur herstellung einer suspension, suspension und deren verwendung |
| EP3387931B1 (de) | 2017-04-10 | 2020-07-15 | ARLANXEO Deutschland GmbH | Vulkanisierbare zusammensetzung enthaltend hxnbr-latex und polyfunktionales epoxid |
| US11370849B2 (en) * | 2018-01-26 | 2022-06-28 | Zeon Corporation | Method for producing carboxy group-containing hydrogenated nitrile rubber |
| WO2019181697A1 (ja) * | 2018-03-22 | 2019-09-26 | 日本ゼオン株式会社 | カルボキシル基含有ニトリルゴムのラテックス中に含まれる、未反応のα，β－エチレン性不飽和ニトリル単量体の回収方法 |
| GB2595599B (en) | 2019-04-08 | 2023-04-19 | Halliburton Energy Services Inc | Stable suspension of elastomer particles for use in a cement slurry |
| CN110396206B (zh) * | 2019-08-22 | 2022-06-14 | 浙江赞昇新材料有限公司 | 一种氢化丁腈橡胶胶乳的制备方法 |
| KR102222870B1 (ko) * | 2019-11-22 | 2021-03-03 | 이창열 | 슬립저항성이 우수한 모노 펌프 고정자용 부틸계 고무 조성물 및 이를 이용하여 제조되는 모노 펌프 고정자 |
| CN111040190A (zh) * | 2019-12-18 | 2020-04-21 | 东营九洲奥华化工有限责任公司 | 一种改性石墨烯丁腈橡胶胶乳及其生产工艺 |
| US20210355366A1 (en) | 2020-05-15 | 2021-11-18 | Halliburton Energy Services, Inc. | Wellbore Servicing Fluid and Methods of Making and Using Same |
| US11680199B2 (en) | 2021-05-14 | 2023-06-20 | Halliburton Energy Services, Inc. | Wellbore servicing fluid and methods of making and using same |
| CN113087983B (zh) * | 2021-05-25 | 2023-04-25 | 黄河三角洲京博化工研究院有限公司 | 一种增强型hnbr材料、其制备方法及应用 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3306871A (en) * | 1959-09-23 | 1967-02-28 | Dow Chemical Co | Synthetic latexes comprising ar-monovinyl aromatic sulfonic acid saltstyrene-butadiene terpolymers |
| DE2830470A1 (de) * | 1978-07-11 | 1980-01-31 | Bayer Ag | Verfahren zur herstellung von emulgatorfreien kautschuklatices |
| CA1220300A (en) | 1982-12-08 | 1987-04-07 | Polysar Limited | Polymer hydrogenation process |
| US4452950A (en) | 1983-02-22 | 1984-06-05 | The Goodyear Tire & Rubber Company | Process for hydrogenation of carbon-carbon double bonds in an unsaturated polymer in latex form |
| JPH0832802B2 (ja) | 1986-02-28 | 1996-03-29 | 日本ゼオン株式会社 | 破断強度に優れた加硫フィルム形成用水性分散体 |
| US5244943A (en) | 1986-02-28 | 1993-09-14 | Nippon Zeon Co., Ltd. | Nitrile group-containing highly saturated polymer rubber latex and process for production thereof |
| DE3618907A1 (de) | 1986-06-05 | 1987-12-10 | Bayer Ag | Verbundwerkstoffe aus vorbehandeltem fasermaterial und vulkanisaten aus hnbr |
| US5077127A (en) | 1987-03-31 | 1991-12-31 | Nippon Zeon Co., Ltd. | Adhesive for bonding rubber to fibers |
| DE3867103D1 (de) | 1987-04-01 | 1992-02-06 | Nippon Zeon Co | Klebstoff zur bindung von gummi an fasern. |
| SU1564674A1 (ru) * | 1987-07-09 | 1990-05-15 | Всесоюзный научно-исследовательский институт нетканых текстильных материалов | Композици св зующего дл изготовлени нетканого материала |
| JP2627554B2 (ja) | 1989-01-31 | 1997-07-09 | 日本ゼオン株式会社 | ポリエステル繊維の処理方法及びポリエステル繊維とニトリル基含有高飽和共重合体ゴムとの接着方法 |
| JP3391116B2 (ja) * | 1994-09-30 | 2003-03-31 | 日本ゼオン株式会社 | ニトリル基含有高飽和共重合体ゴム、その製造方法および加硫性ゴム組成物 |
| US5651995A (en) | 1994-09-30 | 1997-07-29 | Nippon Zeon Co., Ltd. | Highly saturated nitrile rubber, process for producing same, vulcanizable rubber composition, aqueous emulsion and adhesive composition |
| US5539021A (en) * | 1995-06-05 | 1996-07-23 | The Dow Chemical Company | Process for preparing high internal phase ratio emulsions and latexes derived thereof |
| DE19708606A1 (de) | 1997-03-03 | 1998-09-10 | Bayer Ag | Verfahren zur Herstellung von stabilen, feinteiligen Polymerdispersionen |
| CA2538698A1 (en) * | 2003-09-18 | 2005-03-31 | Kaneka Corporation | Process for producing rubbery polymer particle and process for producing resin composition containing the same |
| JP4791725B2 (ja) * | 2004-11-19 | 2011-10-12 | 日本板硝子株式会社 | 歯付ベルトを補強するための補強用シートならびに歯付ベルトおよびその製造方法 |
| JP2006241404A (ja) * | 2005-03-07 | 2006-09-14 | Kaneka Corp | 重合体粒子並びにそれを含む分散体の製造方法 |
| US7411015B2 (en) * | 2005-07-08 | 2008-08-12 | Zeon Chemicals, L.P. | Process for preventing gel formation in lattices of hydrogenated, low molecular weight, functionalized elastomers |
-
2009
- 2009-11-19 EP EP09176534A patent/EP2325237A1/de not_active Withdrawn
-
2010
- 2010-11-10 US US12/943,047 patent/US8642687B2/en active Active
- 2010-11-16 CN CN201010546802.4A patent/CN102070802B/zh active Active
- 2010-11-16 CA CA2721408A patent/CA2721408A1/en not_active Abandoned
- 2010-11-18 EP EP10191637.7A patent/EP2325238B1/de active Active
- 2010-11-18 KR KR1020100114884A patent/KR101818240B1/ko active IP Right Grant
- 2010-11-18 JP JP2010257823A patent/JP5588839B2/ja not_active Expired - Fee Related
- 2010-11-18 TW TW099139629A patent/TWI485188B/zh not_active IP Right Cessation
- 2010-11-18 RU RU2010147029/05A patent/RU2559464C9/ru not_active IP Right Cessation
- 2010-11-19 MX MX2010012609A patent/MX2010012609A/es active IP Right Grant
- 2010-11-19 BR BRPI1004995-9A patent/BRPI1004995A2/pt not_active IP Right Cessation
-
2013
- 2013-12-30 US US14/143,457 patent/US9120918B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US8642687B2 (en) | 2014-02-04 |
| EP2325237A1 (de) | 2011-05-25 |
| CA2721408A1 (en) | 2011-05-19 |
| RU2559464C9 (ru) | 2016-05-27 |
| BRPI1004995A2 (pt) | 2013-03-12 |
| EP2325238A1 (de) | 2011-05-25 |
| EP2325238B1 (de) | 2017-08-30 |
| CN102070802B (zh) | 2015-02-11 |
| MX2010012609A (es) | 2011-08-05 |
| TWI485188B (zh) | 2015-05-21 |
| KR20110055455A (ko) | 2011-05-25 |
| CN102070802A (zh) | 2011-05-25 |
| US20110237717A1 (en) | 2011-09-29 |
| US20140114011A1 (en) | 2014-04-24 |
| KR101818240B1 (ko) | 2018-01-12 |
| RU2559464C2 (ru) | 2015-08-10 |
| US9120918B2 (en) | 2015-09-01 |
| JP2011105939A (ja) | 2011-06-02 |
| RU2010147029A (ru) | 2012-05-27 |
| TW201139524A (en) | 2011-11-16 |
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